| NDC | 58264-0040-1 |
| Set ID | 8a86c0ee-93e9-48da-a7d8-89225e233177 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | DNA Labs, Inc. |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number |
- SPL UNCLASSIFIED SECTION
- INDICATIONS
- INGREDIENTS
- Rx CAUTION
- SUGGESTED DOSAGE
- STORAGE AND HANDLING
- Warnings
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 1 FL. OZ. Bottle Label
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INGREDIENTS AND APPEARANCE
D-40
phosphoric acid, lycopodium clavatum spore, sodium sulfate, claviceps purpurea sclerotium, uranyl nitrate hexahydrate, phaseolus vulgaris whole, and arsenic trioxide solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58264-0040 Route of Administration SUBLINGUAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 12 [hp_X] in 1 mL LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (LYCOPODIUM CLAVATUM SPORE - UNII:C88X29Y479) LYCOPODIUM CLAVATUM SPORE 30 [hp_X] in 1 mL SODIUM SULFATE (UNII: 0YPR65R21J) (Sodium Sulfate Anhydrous - UNII:36KCS0R750) SODIUM SULFATE 12 [hp_X] in 1 mL CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (CLAVICEPS PURPUREA SCLEROTIUM - UNII:01G9XEA93N) CLAVICEPS PURPUREA SCLEROTIUM 4 [hp_X] in 1 mL URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7) URANYL NITRATE HEXAHYDRATE 30 [hp_X] in 1 mL PHASEOLUS VULGARIS WHOLE (UNII: HC262P51WU) (PHASEOLUS VULGARIS WHOLE - UNII:HC262P51WU) PHASEOLUS VULGARIS WHOLE 12 [hp_X] in 1 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 8 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength Alcohol (UNII: 3K9958V90M) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58264-0040-1 29.57 mL in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 01/01/1990 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved homeopathic 01/01/1990 Labeler - DNA Labs, Inc. (031784339)
